Canonical Allele Identifier: CA3892188

Gene: COL12A1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.75095148G>A , CM000668.2:g.75095148G>A	GRCh38
NC_000006.11:g.75804864G>A , CM000668.1:g.75804864G>A	GRCh37
NC_000006.10:g.75861584G>A	NCBI36
NG_042181.1:g.115760C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004370.6:c.8609C>T MANE Select	NP_004361.3:p.Pro2870Leu
ENST00000322507.13:c.8609C>T MANE Select	ENSP00000325146.8:p.Pro2870Leu
NM_004370.5:c.8609C>T	NP_004361.3:p.Pro2870Leu
NM_080645.2:c.5117C>T	NP_542376.2:p.Pro1706Leu
NM_080645.3:c.5117C>T	NP_542376.2:p.Pro1706Leu
ENST00000322507.12:c.8609C>T	ENSP00000325146.8:p.Pro2870Leu
ENST00000345356.10:c.5117C>T	ENSP00000305147.9:p.Pro1706Leu
ENST00000416123.6:c.8381C>T	ENSP00000412864.2:p.Pro2794Leu
ENST00000425443.6:c.1523C>T	ENSP00000399812.2:p.Pro508Leu
ENST00000483888.6:c.8597C>T	ENSP00000421216.1:p.Pro2866Leu
ENST00000511023.1:n.224C>T
ENST00000615798.4:c.5042C>T	ENSP00000483232.1:p.Pro1681Leu
XM_011535434.1:c.8609C>T	XP_011533736.1:p.Pro2870Leu
XM_011535435.1:c.8336C>T	XP_011533737.1:p.Pro2779Leu
XM_011535436.1:c.5117C>T	XP_011533738.1:p.Pro1706Leu
XM_011535436.2:c.5117C>T	XP_011533738.1:p.Pro1706Leu
XM_017010252.2:c.8573C>T	XP_016865741.1:p.Pro2858Leu